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Randomized Controlled Trial
. 2018 Dec 1;3(12):1226-1231.
doi: 10.1001/jamacardio.2018.3957.

Estimated 5-Year Number Needed to Treat to Prevent Cardiovascular Death or Heart Failure Hospitalization With Angiotensin Receptor-Neprilysin Inhibition vs Standard Therapy for Patients With Heart Failure With Reduced Ejection Fraction: An Analysis of Data From the PARADIGM-HF Trial

Affiliations
Randomized Controlled Trial

Estimated 5-Year Number Needed to Treat to Prevent Cardiovascular Death or Heart Failure Hospitalization With Angiotensin Receptor-Neprilysin Inhibition vs Standard Therapy for Patients With Heart Failure With Reduced Ejection Fraction: An Analysis of Data From the PARADIGM-HF Trial

Pratyaksh K Srivastava et al. JAMA Cardiol. .

Abstract

Importance: The addition of receptor-neprilysin inhibition to standard therapy, including a renin-angiotensin system blocker, has been demonstrated to improve outcomes in patients with heart failure with reduced ejection fraction (HFrEF) compared with standard therapy alone. The long-term absolute risk reduction from angiotensin receptor neprilysin inhibitor (ARNI) therapy, and whether it merits widespread use among diverse subpopulations, has not been well described.

Objective: To calculate estimated 5-year number needed to treat (NNT) values overall and for different subpopulations for the Prospective Comparison of ARNI with Angiotensin-Converting Enzyme Inhibitor (ACEI) to Determine Impact on Global Mortality and Morbidity in Heart Failure (PARADIGM-HF) cohort.

Design, setting, and participants: Overall and subpopulation 5-year NNT values were estimated for different end points using data from PARADIGM-HF, a double-blind, randomized trial of sacubitril-valsartan vs enalapril. This multicenter, international study included 8399 men and women with HFrEF (ejection fraction, ≤40%). The study began in December 2009 and ended in March 2014. Analyses began in March 2018.

Interventions: Random assignment to sacubitril-valsartan or enalapril.

Main outcomes and measures: Cardiovascular death or HF hospitalization, cardiovascular death, and all-cause mortality.

Results: The final cohort of 8399 individuals included 1832 women (21.8%) and 5544 white individuals (66.0%), with a mean (SD) age of 63.8 (11.4) years. The 5-year estimated NNT for the primary outcome of cardiovascular death or HF hospitalization with ARNI therapy incremental to ACEI therapy in the overall cohort was 14. The 5-year estimated NNT values were calculated for different clinically relevant subpopulations and ranged from 12 to 19. The 5-year estimated NNT for all-cause mortality in the overall cohort with ARNI incremental to ACEI was 21, with values ranging from 16 to 31 among different subgroups. Compared with imputed placebo, the 5-year estimated NNT for all-cause mortality with ARNI was 11. The 5-year estimated NNT values were also calculated for other HFrEF therapies compared with controls from landmark trials for all-cause mortality and were found to be 18 for ACEI, 24 for angiotensin receptor blockers, 8 for β-blockers, 15 for mineralocorticoid antagonists, 14 for implantable cardioverter defibrillator, and 14 for cardiac resynchronization therapy.

Conclusions and relevance: The 5-year estimated NNT with ARNI therapy incremental to ACEI therapy overall and for clinically relevant subpopulations of patients with HFrEF are comparable with those for well-established HF therapeutics. These data further support guideline recommendations for use of ARNI therapy among eligible patients with HFrEF.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Solomon has received research grants from Alnylam Pharmaceuticals; Amgen; AstraZeneca; Bellerophon Therapeutics; Bristol-Myers Squibb; Celladon; Gilead Sciences; GlaxoSmithKline; Ionis Pharmaceuticals; LoneStar Heart Inc; Mesoblast; MyoKardia; National Institutes of Health/National Heart, Lung, and Blood Institute; Novartis; Sanofi Pasteur; and Theracos and has consulted for Akros, Alnylam Pharmaceuticals, Amgen, AstraZeneca, Bayer, Bristol-Myers Squibb, Corvia Medical, Gilead Sciences, GlaxoSmithKline, Ironwood Pharmaceuticals, Merck & Co, Novartis, Roche, Takeda, Theracos, Quantum Genetics, Cardurion Pharmaceuticals, AoBiome, Janssen, and Cardiac Dimensions. Dr Packer reported consulting for Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, Cardiorentis, Celyad, Daiichi Sankyo, Gilead Sciences, Novartis, Novo Nordisk, Sanofi Pasteur, Takeda, Teva, and ZS Pharma. Dr Roleau reports consulting for AstraZeneca, Bayer, and Novartis. Drs Desai, Zile, and McMuarray report receiving research grants from Novartis. Dr Swedberg reported receiving consulting fees from Novartis, Amgen, and Servier. Dr Fonarow has received research funding from the National Institutes of Health and consulted for Abbott, Amgen, Bayer, Janssen, Medtronic, and Novartis. All other authors report no other relationships relevant to the contents of this paper to disclose.

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